Linked Data
MyVariant Identifiers:
chrX:g.37587286T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37728033T>A , CM000685.2:g.37728033T>A | GRCh38 |
| NC_000023.10:g.37587286T>A , CM000685.1:g.37587286T>A | GRCh37 |
| NC_000023.9:g.37472225T>A | NCBI36 |
| NG_007473.1:g.47174T>A | |
| NG_007473.3:g.47154T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378616.5:c.906T>A MANE Select | ENSP00000367879.3:p.Ile302= | |
| ENST00000378616.3:c.906T>A | ENSP00000367879.3:p.Ile302= | |
| ENST00000465127.1:c.171+302033T>A | ENSP00000417050.1:n.171+302033T>A | |
| NM_021083.2:c.906T>A | NP_066569.1:p.Ile302= | |
| NM_021083.4:c.906T>A MANE Select | NP_066569.1:p.Ile302= |